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Microbial metabolite p-cresol inhibits gut hormone expression and regulates small intestinal transit in mice.
Toft, Pernille Baumann; Vanslette, Amanda Marie; Trost, Kajetan; Moritz, Thomas; Gillum, Matthew Paul; Bäckhed, Fredrik; Arora, Tulika.
Affiliation
  • Toft PB; Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Vanslette AM; Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Trost K; Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Moritz T; Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Gillum MP; Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Bäckhed F; Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Arora T; Wallenberg Laboratory, Department of Molecular and Clinical Medicine, University of Gothenburg, Gothenburg, Sweden.
Front Endocrinol (Lausanne) ; 14: 1200391, 2023.
Article in En | MEDLINE | ID: mdl-37534214
p-cresol is a metabolite produced by microbial metabolism of aromatic amino acid tyrosine. p-cresol and its conjugated forms, p-cresyl sulfate and p-cresyl glucuronide, are uremic toxins that correlate positively with chronic kidney disease and diabetes pathogenesis. However, how p-cresol affects gut hormones is unclear. Here, we expose immortalized GLUTag cells to increasing concentrations of p-cresol and found that p-cresol inhibited Gcg expression and reduced glucagon-like peptide-1 (GLP-1) secretion in vitro. In mice, administration of p-cresol in the drinking water for 2 weeks reduced the transcript levels of Gcg and other gut hormones in the colon; however, it did not affect either fasting or glucose-induced plasma GLP-1 levels. Furthermore, it did not affect glucose tolerance but promoted faster small intestinal transit in mice. Overall, our data suggest that microbial metabolite p-cresol suppresses transcript levels of gut hormones and regulates small intestinal transit in mice.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cresols / Glucagon-Like Peptide 1 Limits: Animals Language: En Journal: Front Endocrinol (Lausanne) Year: 2023 Document type: Article Affiliation country: Denmark Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cresols / Glucagon-Like Peptide 1 Limits: Animals Language: En Journal: Front Endocrinol (Lausanne) Year: 2023 Document type: Article Affiliation country: Denmark Country of publication: Switzerland